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首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >On-line pre-concentration and UV determination of DNA fragments by dynamic coating capillary electrophoresis and its application to detection of genetically modified oilseed rape based on PCR
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On-line pre-concentration and UV determination of DNA fragments by dynamic coating capillary electrophoresis and its application to detection of genetically modified oilseed rape based on PCR

机译:动态包被毛细管电泳在线富集和紫外测定DNA片段及其在基于PCR的转基因油菜检测中的应用

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摘要

In this work, it was demonstrated that on-line pre-concentration and separation of DNA fragments within bared silica column by dynamic coating capillary electrophoresis and UV detection. The DNA fragments were pre-concentrated with long electrokinetic injecting time (99 s), peak height increased dramatically as a function of injection time, especially for shorter length DNA. The concentration sensitivity of DNA fragments can be improved from 20- to 100-fold relative to a normal injection (5 s). The electro-osmotic flow (EOF) and DNA-wall interactions within the capillary were eliminated effectively by dynamic coating method. Employing 0.5% poly(ethylene oxide) (PEO) in Tris-phosphate-EDTA (TBE) buffer as sieving matrix, DNA fragments, ranging from 11 to 657 bp, were separated within 20 min. The linear coefficient of linear relation between the migration and DNA length is 0.999. The DNA fragments amplified from transgenic oilseed rape by polymerase chain reaction (PCR) were separated and detected by this method, demonstrating the potential use of this method for effective DNA analysis and detection of genetically modified organisms (GMO). (C) 2006 Elsevier B.V. All rights reserved.
机译:在这项工作中,通过动态涂层毛细管电泳和UV检测,证明了裸露的硅胶柱中DNA片段的在线预浓缩和分离。 DNA片段经过长时间的电动注入时间(99 s)进行预浓缩,峰高随注入时间而显着增加,特别是对于较短长度的DNA。相对于正常注射(5 s),DNA片段的浓度敏感性可提高20倍至100倍。动态涂层法有效地消除了毛细管内的电渗流(EOF)和DNA-壁相互作用。在Tris-磷酸盐-EDTA(TBE)缓冲液中使用0.5%聚环氧乙烷(PEO)作为筛分基质,在20分钟内分离出11至657 bp的DNA片段。迁移与DNA长度之间线性关系的线性系数为0.999。通过聚合酶链反应(PCR)从转基因油菜中扩增的DNA片段通过此方法进行分离和检测,证明了该方法在有效DNA分析和转基因生物(GMO)检测中的潜在用途。 (C)2006 Elsevier B.V.保留所有权利。

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